Standard

Sphingomyelin (d40:1) levels

near HNRNPA1P67 · rs190671241

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What the study found

Who was studied 4,642 European ancestry women.

The effect Each copy of the G allele shifted the measure 0.559 higher (95% confidence interval 0.4-0.72); p = 4 × 10⁻¹².

Where it sits Chromosome 4, band 4q13.3 — between genes, 98.8 kb from HNRNPA1P67.

What each result means

A/A No copy of the version the research linked to Sphingomyelin (d40:1) levels. This is the starting point the study compared everyone against.

A/G One copy of the version the research linked to Sphingomyelin (d40:1) levels. That is a smaller link than two copies.

G/G Two copies of the version the research linked to Sphingomyelin (d40:1) levels. That is the strongest link of the three results. A link in a study is not a diagnosis.

Source

Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids

Tabassum R, Ruotsalainen S, Ottensmann L, Gerl MJ, Klose C, Tukiainen T, Pirinen M, Simons K, Widén E, Ripatti S

Journal of the American Heart Association · 2022 · PMID 36193934 · open access

Questions about rs190671241

What is rs190671241?

rs190671241 is a single position in the genome, in or near the near HNRNPA1P67 gene. Published research associates it with sphingomyelin (d40:1) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs190671241 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs190671241 come from?

GWAS Catalog, Journal of the American Heart Association 2022, PMID:36193934. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Sphingomyelin (d40:1) levels (rs190671241). MyGeneLog™. https://www.mygenelog.com/variants/rs190671241

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